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细胞毒性 T 细胞异常激活可能是 COVID-19 严重程度的一个决定因素。

Aberrant hyperactivation of cytotoxic T-cell as a potential determinant of COVID-19 severity.

机构信息

Department of Internal Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Department of Anatomy & Cell Biology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; BK21 Plus Biomedical Science Project, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

出版信息

Int J Infect Dis. 2020 Aug;97:313-321. doi: 10.1016/j.ijid.2020.05.106. Epub 2020 May 31.

Abstract

OBJECTIVES

We hypothesized that immune response may contribute to progression of coronavirus disease-19 (COVID-19) at the second week of illness. Therefore, we compared cell-mediated immune (CMI) responses between severe and mild COVID-19 cases.

METHODS

We examined peripheral blood mononuclear cells of laboratory-confirmed COVID-19 patients from their first and third weeks of illness. Severe pneumonia was defined as an oxygen saturation ≤93% at room air. Expressions of molecules related to T-cell activation and functions were analyzed by flow cytometry.

RESULTS

The population dynamics of T cells at the first week were not different between the two groups. However, total numbers of CD4 and CD8 T cells tended to be lower in the severe group at the third week of illness. Expressions of Ki-67, PD-1, perforin, and granzyme B in CD4 or CD8 T cells were significantly higher in the severe group than in the mild group at the third week. In contrast to the mild group, the levels of their expression did not decrease in the severe group.

CONCLUSIONS

Severe COVID-19 had a higher degree of proliferation, activation, and cytotoxicity of T-cells at the late phase of illness without cytotoxic T-cell contraction, which might contribute to the development of severe COVID-19.

摘要

目的

我们假设免疫反应可能导致 COVID-19 疾病的第二周进展。因此,我们比较了重症和轻症 COVID-19 病例的细胞介导免疫(CMI)反应。

方法

我们检测了来自 COVID-19 患者发病第一周和第三周的外周血单核细胞。重症肺炎定义为在室内空气中血氧饱和度≤93%。通过流式细胞术分析与 T 细胞活化和功能相关的分子表达。

结果

两组患者在第一周的 T 细胞群体动力学没有差异。然而,在第三周,重症组的 CD4 和 CD8 T 细胞总数趋于较低。在第三周,重症组 CD4 或 CD8 T 细胞中 Ki-67、PD-1、穿孔素和颗粒酶 B 的表达明显高于轻症组。与轻症组相比,重症组的表达水平没有下降。

结论

重症 COVID-19 在疾病后期具有更高程度的 T 细胞增殖、活化和细胞毒性,而没有细胞毒性 T 细胞收缩,这可能导致重症 COVID-19 的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d1c/7261468/64b31bd51342/gr1_lrg.jpg

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